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- NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_assertion type Assertion NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_head.
- NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_assertion description "[We first screened 153 patients with MR and facial dysmorphism associated with malformations, or growth anomalies, or familial history, with cytogenetically normal chromosomes, and the absence of FRAXA mutation and subtelomeric rearrangements.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.
- NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_assertion evidence source_evidence_literature NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.
- NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_assertion SIO_000772 16773131 NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.
- NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_assertion wasDerivedFrom befree-2016 NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.
- NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_assertion wasGeneratedBy ECO_0000203 NP554496.RAMSQ2bTUUhoffAn0xaZIOOsS9qVB5ulUAKk7c8oXTfWM130_provenance.